| Tag | Content |
|---|
EnhancerAtlas ID | HS113-37540 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:35341150-35342520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:35341634-35341655 | GGAGGAGAAGAACGAGGGAAG | + | 6.15 | | ZNF263 | MA0528.1 | chr9:35341660-35341681 | GGAGGAGGGGAGAGAGTAAGA | + | 7.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 35341177 | 35342200 | | chr9 | 35342400 | 35342489 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I035341 | chr9 | 35341051 | 35342597 |
|
Enhancer Sequence | GTTCCTAATT CTGGATTCTG AAACCATCTT TGGTCTAGAC TTCTGCAATA CAGAGTTCAT 60
CTCAGCTCAC CTAACTTCCC CTCCTTCTCT CGGGTTGTTG CTTTGGCATA GCCTGAGGGA 120
GCTCTTATTT TCCAGTTGAT TCTCTTGTGG TGGTTGTTCA GTAAGAACTG GAATAGATGT 180
CTACTCCAAG AACATGGCAC TGTTTGATTT TAACTGCACT TGATCACTGT ACCTATCCTT 240
CAGCTTTGCC AAATGCTGAC AACAGATTAT ATATACACGA AACCAACCAA CCAACCAACT 300
TAGAGCTTGT CTCAGTAGAA GGGAAGACTC CCTTTGTATT GTGCTCCAGC AGTTCCACGG 360
CTGGCATGCT GTGTTCCGGC TTCCCTCTGA GACTAGGAGC TCCTGAAAGT ATAGGTCTCC 420
ATCTGTGTCT GTTTATATCC TATAGCCCAG ATGTGAGAGA GGTGGATAGG GGAAAAGAAA 480
GCAGGGAGGA GAAGAACGAG GGAAGGAAAT GGAGGAGGGG AGAGAGTAAG ATCTATATTT 540
AGCAAAAGGG AGAGACACTT ACCAAGGGTG TGTGAGTGAG CTTGCTGGCA AGGGTTGTGT 600
GTGCGTGAGT GTGCTGGGAA GGGGGTGTGT GCGCCAGGAA CGTGTGAGGA GGGCTGGTGC 660
CCTATGGGAG GTTGCAGGCA GGAAGCAGCT GGAGAGGAGG AGGAGCAGCA GCAGGAGCAG 720
GAGCTGCCCT GCTTTCTGCC TCAGTCTCAA AGCCCAGAAT CGATTGAGTT AGAATTCCAC 780
ATCCAGTTGA AGTTTGGCTG CTGTTGCCTT CAGCAGGCTG ATCTCAGAAT CCCCCTTGCC 840
AGAGAGGTGT GGACCAGGTT AGATTTCTAC GTTTGCAGCC AGTGAGACTC CTGCCAAGCC 900
CTTCACTGAG GGGTTTTTTT GCAGGGCATT GTTTCTGTCA TCAACTTTGT GCCGTGGAGC 960
CAGCCAGCTG GGTGCAACTG AGAATATTAG CTCCTTGGGT CTGTTTGTCG GTTGGGCAAG 1020
CAGTGGTGCT TTGGCTCAGA AAGTTCGTCC TGTGGCTTCT CTGTCAAACC AAGGAGTGCT 1080
CCTGGATGGA TTTCCTCTTA AAGACAGCAT TTGCCTTCTA AAACTTGAGA ATTCATGGTT 1140
TTAATTTTTT TTTTTAATTT CCTTAACCCT TATTTTGGTT GCAGCAGCAA GGTAAGTGGT 1200
ACCGAGTGTG TATGACTGAC TGAACAACAA GCAGGGCAAA AGGAAAGCAT TTGTGGGTGG 1260
AATATGGAGC AGCTACATTA ATTACGTAAT TGCTTGAGTC AACTTGCTGG TGAGGGGGGT 1320
CATTATAATG AGTGAAAAGT AGCATATGCC GCACTGGGGT AGAATCTTCA 1370
|
